Tetraphenylethylene-based glycoconjugate as a fluorescence "turn-on" sensor for cholera toxin

Chemistry - An Asian Journal

Volumn 6, Issue 9, 2011, Pages 2376-2381

  Hu, Xin Ming ^a,b   Chen, Qi ^a   Wang, Jin Xiang ^a,c   Cheng, Qian Yi ^a   Yan, Chao Guo ^c   Cao, Jie ^d   He, Yu Jian ^b   Han, Bao Hang ^a  

^a NATIONAL CENTER FOR NANOSCIENCE AND TECHNOLOGY   (China)

^b UNIVERSITY OF CHINESE ACADEMY OF SCIENCES   (China)

^c YANGZHOU UNIVERSITY   (China)

^d BEIJING INSTITUTE OF TECHNOLOGY   (China)

Author keywords

aggregation induced emission; cholera toxin; lactose; tetraphenylethylene

Indexed keywords

AGGREGATION-INDUCED EMISSIONS; CARBOHYDRATE-PROTEIN INTERACTIONS; CHOLERA TOXIN; CHOLERA TOXIN B SUBUNIT; CLICK REACTION; GLYCOCONJUGATES; LACTOSE; SPECIFIC INTERACTION; TETRAPHENYLETHYLENE;

FLUORESCENCE; SENSORS; SUGARS;

TOXIC MATERIALS;

CHOLERA TOXIN; DRUG DERIVATIVE; ETHYLENE DERIVATIVE; FLUORESCENT DYE; GLYCOCONJUGATE; LACTOSE; STILBENE DERIVATIVE;

ARTICLE; CHEMISTRY; CONFORMATION; GENETIC PROCEDURES; METHODOLOGY; SPECTROFLUOROMETRY; SYNTHESIS; X RAY CRYSTALLOGRAPHY;

BIOSENSING TECHNIQUES; CHOLERA TOXIN; CRYSTALLOGRAPHY, X-RAY; ETHYLENES; FLUORESCENT DYES; GLYCOCONJUGATES; LACTOSE; MOLECULAR CONFORMATION; SPECTROMETRY, FLUORESCENCE; STILBENES;

EID: 80051722757     PISSN: 18614728     EISSN: 1861471X     Source Type: Journal    
DOI: 10.1002/asia.201100141     Document Type: Article

References (37)

1. D. A. Sack, R. B. Sack, G. B. Nair, A. K. Siddique, Lancet 2004, 363, 223-233.
2. J. A. Mertz, J. A. McCann, W. D. Picking, Biochem. Biophys. Res. Commun. 1996, 226, 140-144
3. I. Vrasidas, N. J. de Mol, R. M. J. Liskamp, R. J. Pieters, Eur. J. Org. Chem. 2001, 4685-4692
4. C. L. Schofield, R. A. Field, D. A. Russell, Anal. Chem. 2007, 79, 1356-1361.
5. E. A. Merritt, W. G. J. Hol, Curr. Opin. Struct. Biol. 1995, 5, 165-171
6. E. A. Merritt, S. Sarfaty, F. Vandenakker, C. Lhoir, J. A. Martial, W. G. J. Hol, Protein Sci. 1994, 3, 166-175
7. W. B. Turnbull, B. L. Precious, S. W. Homans, J. Am. Chem. Soc. 2004, 126, 1047-1054.
8. H. Lis, N. Sharon, Chem. Rev. 1998, 98, 637-674
9. M. Mammen, S.-K. Choi, G. M. Whitesides, Angew. Chem. 1998, 110, 2908-2953
10. Angew. Chem. Int. Ed. 1998, 37, 2754-2794
11. R. Jelinek, S. Kolusheva, Chem. Rev. 2004, 104, 5987-6015.
12. Y. C. Lee, R. T. Lee, Acc. Chem. Res. 1995, 28, 321-327.
13. J. J. Lundquist, E. J. Toone, Chem. Rev. 2002, 102, 555-578.
14. J. D. Luo, Z. L. Xie, J. W. Y. Lam, L. Cheng, H. Y. Chen, C. F. Qiu, H. S. Kwok, X. W. Zhan, Y. Q. Liu, D. B. Zhu, B. Z. Tang, Chem. Commun. 2001, 1740-1741
15. K. Hatano, H. Saeki, H. Yokota, H. Aizawa, T. Koyama, K. Matsuoka, D. Terunuma, Tetrahedron Lett. 2009, 50, 5816-5819
16. Y. N. Hong, J. W. Y. Lam, B. Z. Tang, Chem. Commun. 2009, 4332-4353
17. M. Wang, G. X. Zhang, D. Q. Zhang, D. B. Zhu, B. Z. Tang, J. Mater. Chem. 2010, 20, 1858-1867.
18. A. J. Qin, J. W. Y. Lam, L. Tang, C. K. W. Jim, H. Zhao, J. Z. Sun, B. Z. Tang, Macromolecules 2009, 42, 1421-1424.
19. H. Tong, Y. N. Hong, Y. Q. Dong, M. Haussler, J. W. Y. Lam, Z. Li, Z. F. Guo, Z. H. Guo, B. Z. Tang, Chem. Commun. 2006, 3705-3707.
20. Y. Q. Dong, J. W. Y. Lam, A. J. Qin, J. Z. Liu, Z. Li, B. Z. Tang, Appl. Phys. Lett. 2007, 91, 011111
21. L. Liu, G. X. Zhang, J. F. Xiang, D. Q. Zhang, D. B. Zhu, Org. Lett. 2008, 10, 4581-4584.
22. H. Tong, Y. N. Hong, Y. Q. Dong, M. Haeussler, Z. Li, J. W. Y. Lam, Y. P. Dong, H. H. Y. Sung, I. D. Williams, B. Z. Tang, J. Phys. Chem. B 2007, 111, 11817-11823
23. Y. N. Hong, M. Haussler, J. W. Y. Lam, Z. Li, K. K. Sin, Y. Q. Dong, H. Tong, J. Z. Liu, A. J. Qin, R. Renneberg, B. Z. Tang, Chem. Eur. J. 2008, 14, 6428-6437
24. M. Wang, X. G. Gu, G. X. Zhang, D. Q. Zhang, D. B. Zhu, Anal. Chem. 2009, 81, 4444-4449
25. Q. Chen, N. Bian, C. Cao, X.-L. Qiu, A.-D. Qi, B.-H. Han, Chem. Commun. 2010, 46, 4067-4069
26. T. Kato, A. Kawaguchi, K. Nagata, K. Hatanaka, Biochem. Biophys. Res. Commun. 2010, 394, 200-204
27. T. Sanji, K. Shiraishi, M. Nakamura, M. Tanaka, Chem. Asian J. 2010, 5, 817-824
28. K. Shiraishi, T. Sanji, M. Tanaka, Tetrahedron Lett. 2010, 51, 6331-6333.
29. J. E. McMurry, Chem. Rev. 1989, 89, 1513-1524.
30. H. C. Kolb, M. G. Finn, K. B. Sharpless, Angew. Chem. 2001, 113, 2056-2075
31. Angew. Chem. Int. Ed. 2001, 40, 2004-2021
32. V. V. Rostovtsev, L. G. Green, V. V. Fokin, K. B. Sharpless, Angew. Chem. 2002, 114, 2708-2711
33. Angew. Chem. Int. Ed. 2002, 41, 2596-2599.
34. F. D. Tropper, F. O. Andersson, S. Braun, R. Roy, Synthesis 1992, 618-620.
35. H. Chen, Y. Zheng, J.-H. Jiang, H.-L. Wu, G.-L. Shen, R.-Q. Yu, Biosens. Bioelectron. 2008, 24, 684-689
36. M. Labib, M. Hedström, M. Amin, B. Mattiasson, Anal. Chim. Acta 2009, 634, 255-261
37. S.-H. Tark, A. Das, S. Sligar, V. P. Dravid, Nanotechnology 2010, 21, 435502.